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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440413Generated: October 27, 2026

Water → 4-(3,5-di-tertiary-butyl-4-hydroxy-N-methylanilino)benzoic acid

https://huagongshe.com/reaction/1440413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant4-(3,5-Di-tertiary-butyl-4-hydroxyanilino)benzoic acidHCID 13960406—
SolventMethyl iodideHCID 6328—
Product4-(3,5-di-tertiary-butyl-4-hydroxy-N-methylanilino)benzoic acidHCID 22401583—

Reaction Steps

A solution of 3.4 g (0.010 mole) of 4-(3,5-di-tertiary-butyl-4-hydroxyanilino)benzoic acid (prepared in Example 1) in 35 ml of N,N-dimethylformamide and 3.5 ml of methyl iodide was heated at 95° C. for about 48 hours under nitrogen. The reaction mixture was poured into cold water and the resulting solid was collected and then taken up in chloroform. The chloroform solution was filtered, washed with water, dried with magnesium sulfate and evaporated to give a tan solid. This material was recrystallized first from benzene and then from a mixture of ethanol and water to give 1.5 g of white crystalline 4-(3,5-di-tertiary-butyl-4-hydroxy-N-methylanilino)benzoic acid, m.p. 240°-244° C. Analysis: Calculated for C22H29NO3 : % C, 74.3; % H, 8.2; % N, 3.9. Found: % C, 74.4; % H, 8.3; % N, 3.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498745
Source datasetuspto-grants-1996_03
ORD IDord-78b02402a7e94c9ca1611ad64bb11f27
Source noteuspto-grants-1996_03